Triad Group, a manufacturer of over-the-counter products has initiated a voluntary product recall involving all lots of Alcohol Prep Pads, Alcohol Swabs or Alcohol Swabsticks manufactured by Triad Group which may be included in a variety of other products labeled with other manufacturers' names.
Keys Manufacturing Company, Inc. of Paris, IL is recalling Pig Ears for Pet Treats because it has the potential to be contaminated with Salmonella.
American Regent is conducting a nationwide voluntary recall of Ammonium Molybdate Injection, USP (Molybdenum 250mcg/10mL) 10mL Single Dose Vial NDC 0517-6610-25, Lot # 9409, Exp. Date June 2011. This recall was initiated on April 26, 2011 to the User Level for Lot # 9409 only. No other lots of Ammonium Molybdate Injection, USP are subject to this recall.
Greenstone LLC announced a recall of medicines with lot number FI0510058-A on the label. Bottles labeled as Citalopram (used to treat depression) may contain Finasteride (used for the treatment of benign prostatic hyperplasia).
H&P industries, Inc., a manufacturer of over-the-counter products has initiated a voluntary product recall of all lots of Povidine Prep Pads manufactured by H&P Industries, Inc. but which are private labeled for many accounts.
The Food and Drug Administration’s Center for Veterinary Medicine (CVM) has become aware of a human drug recall for Phenobarbital tablets. Phenobarbital is prescribed by veterinarians as an extralabel use for treating seizures in animals.
This recall was initiated because some of the vials of these lots may contain visible particulates. Potential adverse events after intravenous administration of solutions containing particulates may include disruption of blood flow within small blood vessels in the lung, localized inflammation (swelling and redness due to accumulation of inflammatory cells), and granuloma formation.
American Regent is conducting a nationwide voluntary recall of specific Dexamethasone Sodium Phosphate Injections.
Jones Natural Chews Co of Rockford, IL is recalling 2705 boxes of Pig Ears because it has the potential to be contaminated with Salmonella.
At its July 23rd meeting, the OVMEB voted to rescind the proposed rule changes regarding exams and vaccines. The current rules remain in effect.
WellPet LLC has voluntarily recalled certain lots of Wellness® canned cat food due to the possibility that they contain less than adequate levels of thiamine (Vitamin B1).
American Regent is recalling one lot of Potassium Phosphates Injection, USP, 15 mM/5 mL Phosphorus; 22 mEq/5 mL Potassium, 5 mL Single Dose Vial.
American Regent is recalling One Lot of Sodium Thiosulfate Injection, USP, 10% (100 mg/mL), 10 mL Single Dose Vial due to particulate contamination.
The Food and Drug Administration (FDA) announced today an anticipated shortage of Vetsulin (porcine insulin zinc suspension), a product used to treat diabetes mellitus in dogs and cats. Vetsulin is manufactured by Intervet/Schering-Plough Animal Health and is only available to animals currently enrolled in the Vetsulin Critical Need Program.
Manna Pro Products, LLC is voluntarily recalling a single lot (1006) of Family Farm Complete Horse 10 horse feed, UPC 0 95668 90151 6, packaged in 40 lb. bags because it may contain monensin sodium (Rumensin). Monensin sodium is a medication approved for use in some livestock and poultry species, but can be fatal to horses if fed at sufficiently high levels.
Merrick Pet Care, Inc. of Amarillo, Texas is recalling the Jr. Texas Taffy pet treat (ITEM # 27077, UPC # 02280827077, All Lots up to and including 10364) because they have the potential to be contaminated with Salmonella.
Teva Pharmaceuticals is recalling Metronidazole Tablets USP, 250mg, lot 312566, expiration date 05/2012. This product lot is being recalled due to the presence of underweight tablets.
American Regent is conducting a nationwide voluntary recall to the consumer and user level of ALL unexpired lots of the following products: Sodium Bicarbonate Injection, USP, 7.5%, 44.6 mEq/50 mL, Single Dose Vial NDC # 0517-0639-25 and Sodium Bicarbonate Injection, USP, 8.4%, 50 mEq/50 mL, Single Dose Vial NDC # 0517-1550-25.
American Regent is conducting a nationwide voluntary recall of the following: Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL, 30 mL Multiple Dose Vial, NDC # 0517-4930-25.
B. Braun is recalling seven lots of heparin injection products. Testing of retained crude heparin samples indicated a trace amount of oversulfated chondroitin sulfate (OSCS) contaminant.
The following recall is being posted as some veterinarians may use this product in treating their patients. Sandoz is initiating this voluntary recall of all 24 lots of the affected product following the finding of small glass flakes in a limited number of vials in four lots.
The Food and Drug Administration (FDA) announced the addition of a boxed warning to the label of two METACAM® (meloxicam) products.
Actavis Inc. has recalled at the wholesale and retail levels only 18 lots of Fentanyl Transdermal System 25 mcg/hour C-II patches manufactured for Actavis by Corium International in the United States.